29443-47-8

Basic information

• Product Name: Cyclohexane, 1,1-diiodo-
• CAS NO: 29443-47-8
• Molecular Formula: C6H10I2
• Molecular Weight: 335.954
• Mol File: 29443-47-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Cyclohexane, 1,1-diiodo-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexane, 1,1-diiodo-(29443-47-8)
• EPA Substance Registry System: Cyclohexane, 1,1-diiodo-(29443-47-8)

Safety Data

• Hazardous Substances Data: 29443-47-8(Hazardous Substances Data)

Upstream product

• 6156-08-7 cyclohexanone hydrazone 
• 29026-66-2 spiro<1,3-benzoxathiole-2,1'-cyclohexane> 
• 75-36-5 acetyl chloride 
• 182-55-8 spiro[benzo[d][1,3]dioxole-2,1'-cyclohexane] 

Downstream Products

• 371-90-4 1,1-difluorocyclohexane 

Relevant articles and documents

Studies on the Synthesis of Heterocyclic Compounds. XVI. Cleavage of 1,3-Benzodioxoles and -Benzoxathioles by Sodium Iodide-Acyl Chloride

The cleavage reaction of ethereal and thioethereal bonds with sodium iodide and acyl chloride has been studied.In all the 1,3-benzodioxoles and -benzoxathioles studied, the opening of the heterocyclic ring with formation of 1,2-diacetoxybenzene or 2-hydroxythiophenol diacetic acid ester and gem-diiodoalkanes and iodoalkenes has been observed.The structure of newly prepared compounds has been determined by analytical and spectroscopic data or comparison with authentic samples.

A MILD, CONVENIENT, HALOGEN-EXCHANGE ROUTE TO GEM-DIFLUORIDES AND TRIFLUORIDES

Reaction of gem-dihalides R1R2CX2 (X=Cl or I) and of PhCCl3 with AgBF4 at room or sub-ambient temperatures affords the corresponding gem-difluorides and trifluoride in unoptimised yields of 35-84percent.